[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"clabsi---central-line-associated-bloodstream-infection\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:clabsi---central-line-associated-bloodstream-infection":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,6,0,[8,53,88,109,136,160],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":31,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":52},"100640493","neonatal-catheter-lock-for-infection-prevention-100640493",false,"NCT07585188","Neonatal Catheter Lock for Infection Prevention","Taurolidine Lock for Prevention of Central-Line Associated Bloodstream Infections in Neonates: A Triple-blind Randomized Controlled Trial","Neo-CLIP","Inclusion Criteria:\n\n* presence of a CVC (ECC, CICC, or FICC) for at least 48 hours\n* absence of systemic antibiotic therapy in the 48 hours preceding enrollment\n\nExclusion Criteria:\n\n* presence of an umbilical venous catheter\n* suspected thrombophilic disorder","ALL","1 Day","120 Days",{"count":21,"type":22},576,"ESTIMATED","INTERVENTIONAL",[25],"NA","For newborns admitted to Neonatal Intensive Care Units (NICUs), one of the main risk factors for late-onset sepsis is the presence of a central venous catheter (CVC), which is often essential for the administration of medications and parenteral nutrition in this patient population. From a nosological perspective, sepsis associated with the presence of a venous catheter is defined by two acronyms: CRBSI (Catheter-Related Bloodstream Infection - a microbiological definition) and CLABSI (Central Line-Associated Bloodstream Infection - an epidemiological definition).\n\nAmong preventive strategies for CRBSI\u002FCLABSI, antibiotic or antimicrobial catheter lock solutions - instilled in a volume equivalent to the catheter dead space and retained within the lumen until the next use - have demonstrated favorable efficacy in reducing infection risk.\n\nTaurolidine 2% is considered a preferred agent due to its broad-spectrum antibacterial and antifungal activity and its lack of association with the development of antimicrobial resistance.\n\nHowever, its prophylactic use in neonates remains largely investigational, with current evidence limited to small, retrospective observational studies involving catheters ≥3 Fr (e.g., femoral inserted central catheters - FICCs, centrally inserted central catheters - CICCs, and umbilical venous catheters).\n\nIn NICUs, epicutaneo-caval catheters (ECCs) are the most commonly used central venous access devices and represent a major source of catheter-related infections. Despite this, the use of antimicrobial lock prophylaxis in ECCs has been limited by concerns regarding catheter occlusion, given their smaller diameter (≤2 Fr). Nevertheless, available evidence indicates that short-duration locks, when combined with meticulous infusion line management, can be safely implemented without increasing the risk of catheter occlusion.\n\nThe aim of the study is to evaluate the efficacy of 2% taurolidine lock in the prevention of CLABSI\u002FCRBSI in neonates with CVC (ECC, FICC, or CICC).",[28,29,30],"CLABSI - Central Line Associated Bloodstream Infection","CRBSI - Catheter Related Bloodstream Infection","Neonatal Sepsis, Late-Onset",[32,33,34,35,36,37,38,39],"Taurolidine","Catheter lock therapy","Epicutaneo-caval catheter","Femoral inserted central catheters","Centrally inserted central catheters","Neonatal Intensive Care Unit","Newborn","Parenteral nutrition","NOT_YET_RECRUITING","2026-05-08",{"date":43,"type":44},"2026-05-13","ACTUAL",{"date":46,"type":22},"2026-10",{"date":48,"type":22},"2029-10",{"name":50,"class":51},"University of Turin, Italy","OTHER",1,{"id":54,"slug":55,"hasResults":11,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":59,"eligibilityCriteria":60,"healthyVolunteers":11,"sex":17,"minAge":61,"maxAge":4,"enrollmentInfo":62,"targetDuration":4,"studyType":64,"phases":4,"briefSummary":65,"conditions":66,"keywords":75,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":79,"lastUpdatePostDateStruct":80,"startDateStruct":82,"completionDateStruct":84,"leadSponsor":86,"locationsCount":52},"100624164","duke-virtual-integrated-workflow-100624164","NCT07406074","Duke Virtual IntEgrated Workflow","DUH Innovation Units","Duke VIEW","Inclusion Criteria:\n\n* Admission to the hospital on one of six clinical units\n\nExclusion Criteria:\n\n* Less than 18 years old","18 Years",{"count":63,"type":22},10000,"OBSERVATIONAL","This quality improvement initiative aims to evaluate the implementation, utilization, and impact of virtual care technologies and workflows being implemented at Duke University Health System (DUHS). This project is embedded within operational workflows and is designed to inform strategic decision-making and resource allocation. The evaluation will focus on key performance indicators (KPIs) relevant to hospital operations and patient outcomes, including but not limited to: Length of Stay, Readmission Rates, Patient Satisfaction Scores, and Other Quality and Safety Metrics. These KPIs will be evaluated across three clinical units at Duke University Hospital, in which virtual care technologies are being implemented. These will be compared to three control units of similar characteristics. Differences in KPIs will be examined across all units over 12 months.",[67,68,28,69,70,71,72,73,74],"Falls Injury","Readmission Rates","Catheter Associated Urinary Tract Infection","Hospital Acquired Pressure Injury","Venous Thromboembolism (VTE)","Nurses","Satisfaction, Patient","Length of Stay",[76,77,78],"Virtual Care","Nursing","Inpatient","2026-02-09",{"date":81,"type":44},"2026-02-12",{"date":83,"type":22},"2026-02-04",{"date":85,"type":22},"2027-02-03",{"name":87,"class":51},"Duke University",{"id":89,"slug":90,"hasResults":11,"nctId":91,"briefTitle":92,"officialTitle":93,"acronym":4,"eligibilityCriteria":94,"healthyVolunteers":11,"sex":17,"minAge":61,"maxAge":4,"enrollmentInfo":95,"targetDuration":4,"studyType":64,"phases":4,"briefSummary":97,"conditions":98,"keywords":4,"overallStatus":99,"whyStopped":4,"lastUpdateSubmitDate":100,"lastUpdatePostDateStruct":101,"startDateStruct":103,"completionDateStruct":105,"leadSponsor":107,"locationsCount":52},"100612555","epidemiological-investigation-of-central-venous-catheter-related-bloodstream-infections-in-icus-in-china-100612555","NCT07255105","Epidemiological Investigation of Central Venous Catheter-related Bloodstream Infections in Icus in China","The First Phase of the Closed-loop Improvement Project for Preventing CLABSI","Inclusion Criteria:\n\n* 1\\. Admitted to the ICU with a central venous catheter placed in place and the expected indwelling time exceeds 48 hours (including newly placed central venous catheters or the continued indwelling of existing qualified central venous catheters)\n\n  2\\. Patients aged 18 or above\n\n  3\\. Sign the informed consent form\n\nExclusion Criteria:\n\n1. Patients who have had a central venous catheter indwelled for more than 24 hours before being admitted to the ICU (and are not going to have it replaced immediately)\n2. Patients who were re-admitted to the ICU during the study period\n3. Lactating and pregnant women",{"count":96,"type":22},1846,"In recent years, with the rapid advancement of medical technology and the rapid development of critical care medicine, the use of various central venous catheters in icus has been increasing day by day. Central venous catheter-related bloodstream infection (CLABSI), as a common catheter complication, preventable nosocomial acquired infections have gradually become a focus of attention in the ICU. Once CLABSI occurs, it often leads to a mortality rate as high as 28% to 30% for patients. Data from our country shows that patients with CLASBI will have their hospital stay extended by 8 to 13 days. The additional cost has increased by 3,500 US dollars.\n\nTherefore, over the years, medical systems both at home and abroad have been committed to the prevention and control of CLABSI. The incidence of CLABSI in icus in the United States in 2020 was 0.87 per thousand catheter days. In 2018, the incidence rate of CLABSI in 79 icus in China was 1.5 per thousand catheter days. All the above incidence rates have decreased significantly compared with previous data.\n\nDuring the COVID-19 pandemic in 2020, the global healthcare system faced severe challenges. Particularly, factors such as the aggravation of patients' conditions in icus, the sharp increase in the use of central venous catheters, the shortage of medical staff, and the ineffective implementation of CLABSI prevention measures jointly led to a significant increase in the incidence of CLABSI. The number of CLABSI cases recorded by the US NHSN in the fourth quarter increased by as much as 47%. In response to this crisis, international and domestic authoritative institutions responded promptly: In 2022, the American Society of Epidemiology (SHEA) updated its prevention strategy for CLABSI. In the same year, the National Health Commission of China emphasized in its medical quality improvement goals the need to reduce intravascular catheter-related infections, especially in the field of critical care medicine, and explicitly indicated the need to lower the incidence of CLABSI in icus.\n\nHowever, at present, there is still no large-scale investigation on the incidence of CLABSI after COVID-19 in Chinese mainland. This is related to the fact that there is no standard data collection and monitoring platform at present, and the judgment standards and capabilities of various medical institutions are inconsistent.\n\nThis study took adult patients with central venous catheters in icus across the country as the research subjects. Through a prospective cohort study, the current incidence and related influencing factors of CLABSI were clarified. To provide a basis and reference for further formulating and implementing CLBASI prevention strategies in the future.",[28],"RECRUITING","2025-11-19",{"date":102,"type":44},"2025-11-28",{"date":104,"type":44},"2025-06-08",{"date":106,"type":22},"2026-09-30",{"name":108,"class":51},"Jianfeng Xie",{"id":110,"slug":111,"hasResults":11,"nctId":112,"briefTitle":113,"officialTitle":114,"acronym":4,"eligibilityCriteria":115,"healthyVolunteers":116,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":117,"targetDuration":4,"studyType":23,"phases":119,"briefSummary":120,"conditions":121,"keywords":4,"overallStatus":99,"whyStopped":4,"lastUpdateSubmitDate":127,"lastUpdatePostDateStruct":128,"startDateStruct":130,"completionDateStruct":132,"leadSponsor":134,"locationsCount":52},"100522674","multicenter-clinical-translational-study-of-icu-no-crbsi-based-on-improvement-science-100522674","NCT06085690","Multicenter Clinical Translational Study of \"ICU-NO CRBSI\" Based on Improvement Science","A Multicenter Clinical Translational Study of \"ICU-NO CRBSI\" Based on Improvement Science in China","Inclusion Criteria:\n\n* ICU stay over 48 hours\n* CVC was placed for more than 24 hours\n\nExclusion Criteria:\n\n* Pregnant patients\n* Patients with a history of CRBSI infection\n* Patients with central venous catheterization were brought in from other hospitals",true,{"count":118,"type":22},8050,[25],"The goal of this type of study is to construct the continuous quality promotion project \"ICU-NO CRBSI(Catheter-Related Bloodstream Infection , CRBSI)\" based on improvement science, and to verify its effect in the prevention of central venous catheter-related bloodstream infection and continuous quality improvement in ICU ( Intensive Care Unit , ICU) through multi-center implementation and two rounds of improvement.\n\nThe main question\\[s\\] it aims to answer are:\n\nWhat is the incidence of catheter-related bloodstream infection in the ICU of participating units? How compliant are health care providers in the ICU with evidence-based sensory control practices for the prevention of catheter-associated bloodstream infection?\n\nParticipants will be provided with the hospital's routine CVC (Central Venous Catheter ,CVC) care practices and CVC quality improvement measures based on evidence-based guidelines What technical and cultural support is needed to implement quality and safety improvement measures?",[29,122,123,124,125,28,126],"Evidence-based Nursing Practice","Central Venous Catheter Related Bloodstream Infection","Central Venous Catheter Associated Bloodstream Infection","Central Line Infection","Quality Improvement","2025-11-14",{"date":129,"type":44},"2025-11-17",{"date":131,"type":44},"2023-09-04",{"date":133,"type":22},"2025-12-31",{"name":135,"class":51},"Fudan University",{"id":137,"slug":138,"hasResults":11,"nctId":139,"briefTitle":140,"officialTitle":140,"acronym":4,"eligibilityCriteria":141,"healthyVolunteers":11,"sex":17,"minAge":142,"maxAge":143,"enrollmentInfo":144,"targetDuration":146,"studyType":64,"phases":4,"briefSummary":147,"conditions":148,"keywords":4,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":151,"lastUpdatePostDateStruct":152,"startDateStruct":154,"completionDateStruct":156,"leadSponsor":158,"locationsCount":4},"100609062","umbilical-venous-versus-peripherally-inserted-central-catheters-in-neonates-a-prospective-cohort-study-of-complications-catheter-survival-and-clabsi-100609062","NCT07209670","Umbilical Venous Versus Peripherally Inserted Central Catheters in Neonates: A Prospective Cohort Study of Complications, Catheter Survival, and CLABSI\"","Inclusion Criteria:\n\n* Neonates admitted to the neonatal intensive care unit (NICU) requiring central venous access.\n\n  * Infants in whom either an umbilical venous catheter (UVC) or a peripherally inserted central catheter (PICC) was inserted for clinical indications (Parenteral nutrition, administration of intravenous medications (e.g., antibiotics, inotropes, anticonvulsants, fluids) and blood sampling for frequent labs, especially in critically ill neonates).\n  * Catheter insertion performed within the first 28 days of life.\n\nExclusion Criteria:\n\n* Neonates with major congenital anomalies (e.g.abdominal wall defects) that may interfere with catheter placement or outcomes.\n* Insertion site infection\n* Infants with severe coagulopathy or bleeding disorders contraindicating central catheter insertion.\n* Neonates who received both UVC and PICC simultaneously during the same admission.\n* Cases with incomplete clinical records or missing follow-up data.","0 Days","28 Days",{"count":145,"type":22},360,"1 Year","This study aims to prospectively compare umbilical venous catheters (UVCs) and peripherally inserted central catheters (PICCs) in neonates, focusing on complications, catheter survival, and central line-associated bloodstream infection (CLABSI) rates",[149,150,28],"Peripherally Inserted Central Catheter","Umbilical Venous Catheter","2025-09-29",{"date":153,"type":44},"2025-10-07",{"date":155,"type":22},"2025-12-01",{"date":157,"type":22},"2028-12-20",{"name":159,"class":51},"Assiut University",{"id":161,"slug":162,"hasResults":11,"nctId":163,"briefTitle":164,"officialTitle":165,"acronym":4,"eligibilityCriteria":166,"healthyVolunteers":11,"sex":17,"minAge":61,"maxAge":4,"enrollmentInfo":167,"targetDuration":4,"studyType":23,"phases":169,"briefSummary":170,"conditions":171,"keywords":4,"overallStatus":99,"whyStopped":4,"lastUpdateSubmitDate":177,"lastUpdatePostDateStruct":178,"startDateStruct":180,"completionDateStruct":182,"leadSponsor":184,"locationsCount":52},"100544180","tunneled-peripherally-inserted-central-catheter-picc-in-adult-patients-and-associated-outcomes-100544180","NCT06365528","Tunneled Peripherally Inserted Central Catheter (PICC) in Adult Patients and Associated Outcomes","Tunneled Versus Non-Tunneled Peripherally Inserted Central Catheter and Their Effects on Reducing Combined or Isolated Outcomes (Obstruction, Infection, Thrombosis, and Dislodgement): Multicenter Randomized Clinical Trial","Inclusion Criteria:\n\n* adult patients (\\>= 18 years old) admitted to medical clinics, surgical clinics, or ICU, who have an indication for PICC insertion;\n\nExclusion Criteria:\n\n* patients with Chronic Kidney Disease, whether dialytic or not;\n* patients in critical or unstable condition characterized by the need for intubation, respiratory rate \\\u003C8 or \\>35 breaths per minute, oxygen saturation \\\u003C90%, heart rate \\\u003C40 or \\>140 beats per minute, systolic blood pressure \\\u003C90mmHg, decreased Glasgow Coma Scale \\>2 points, or prolonged (\\>5 minutes) or repeated seizures;\n* patients with cognitive deficits that impair their understanding of the study and do not have a responsible party to assist in this stage.",{"count":168,"type":22},840,[25],"The aim of this multicenter randomized clinical trial is to compare the tunneling technique of PICC insertion with the non-tunneled insertion technique in the incidence of the combined or isolated outcome of catheter-related bloodstream primary infection, thrombosis, obstruction, and accidental dislodgement in the adult population within a period of up to 30 days.",[28,172,173,174,175,176],"Deep Vein Thrombosis","Dislodged Catheter","Occlusion","Catheter Rupture","Catheter (Other); Complications","2024-05-16",{"date":179,"type":44},"2024-05-20",{"date":181,"type":44},"2024-05-06",{"date":183,"type":22},"2026-07-31",{"name":185,"class":51},"Hospital de Clinicas de Porto Alegre"]